Colin Bishop

A novel gene, Pog, is necessary for primordial germ cell proliferation in the mouse and underlies the germ cell deficient mutation, gcd.

Mouse GGN1 and GGN3, two germ cell-specific proteins from the single gene Ggn, interact with mouse POG and play a role in spermatogenesis.

Deletion of the Parkin coregulated gene causes male sterility in the quaking(viable) mouse mutant.

Sox9 is sufficient for functional testis development producing fertile male mice in the absence of Sry.

A deletion in the gene encoding sphingomyelin phosphodiesterase 3 (Smpd3) results in osteogenesis and dentinogenesis imperfecta in the mouse.

UTP14c is a recently acquired retrogene associated with spermatogenesis and fertility in man.

Generation of rat mutants using a coat color-tagged Sleeping Beauty transposon system.

Three loci on mouse chromosome 5 and 10 modulate sex determination in XX Ods/+ mice.

Developmental expression and gene regulation of insulin-like 3 receptor RXFP2 in mouse male reproductive organs.

Oocyte-specific G-protein-coupled receptor 3 (GPR3): no perturbations found in 82 women with premature ovarian failure (first report).

A mutation in the inner mitochondrial membrane peptidase 2-like gene (Immp2l) affects mitochondrial function and impairs fertility in mice.

Reprogramming of human somatic cells using human and animal oocytes.

Spermatogenesis associated retrogenes are expressed in the human ovary and ovarian cancers.

The role of the mouse y chromosome on susceptibility to testicular germ cell tumors.

Reprogramming human fibroblasts using HIV-1 TAT recombinant proteins OCT4, SOX2, KLF4 and c-MYC.

Bladder dysfunction in a new mutant mouse model with increased superoxide--lack of nitric oxide?

Cloned, CD117 selected human amniotic fluid stem cells are capable of modulating the immune response.

Oxidative stress is involved in age-dependent spermatogenic damage of Immp2l mutant mice.

Mex3c mutation reduces adiposity and increases energy expenditure.

Nicotinamide mononucleotide adenylyltransferase 2 (Nmnat2) regulates axon integrity in the mouse embryo.

Lack of nicotinamide mononucleotide adenylyltransferase 2 (Nmnat2): consequences for mouse bladder development and function.

Amniotic fluid stem cells improve survival and enhance repair of damaged intestine in necrotising enterocolitis via a COX-2 dependent mechanism.

Novel frem1-related mouse phenotypes and evidence of genetic interactions with gata4 and slit3.

TALEN-mediated modification of the bovine genome for large-scale production of human serum albumin.

A hydrogel bioink toolkit for mimicking native tissue biochemical and mechanical properties in bioprinted tissue constructs.

A liver-on-a-chip platform with bioprinted hepatic spheroids.